A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151713



Internal ID18855807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:18990613..18993914hg38UCSC Ensembl
OuterchrY:21152499..21155800hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg383302
hg193302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003139
SamplesKWB1
Known GenesCD24, TTTY14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151713
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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